Answer:
a. 21.7824 g
b. 0.2362 g
c. 31.5273 g
Please see the answers in the picture attached below.
Explanation:
Please see the step-by-step solution in the picture attached below.
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Correct Question: what is the oxidizing agent in the reaction.
2MnO4–(aq) +10Cl–(aq) + 16H+(aq) --------> 5Cl2(g) + 2Mn2+(aq) +8H2O(l)
Answer: MnO4-is the oxidizing agent
Explanation:
In the reaction 2MnO4–(aq) +10Cl–(aq) + 16H+(aq) --------> 5Cl2(g) + 2Mn2+(aq) +8H2O(l)
Oxidizing agent oxidizes other molecules while the themselves get reduced.
oxidizing agents give away Oxygen to other compounds.
MnO4-is the oxidizing agent because
On the reactants side
Oxidation number of Mn in 2MnO4- is +7
Oxidation number of Cl- is -1
On the products side
Oxidation number of Mn is +2
While oxidation number of Cl is zero
Therefore the oxidizing agent is 2MnO4 because is oxidizes Chlorine from -1 to 0 while itself got reduced from oxidation state of +7 to +2
Answer:
The precipitate is CuS.
Sulfide will precipitate at [S2-]= 3.61*10^-35 M
Explanation:
<u>Step 1: </u>Data given
The solution contains 0.036 M Cu2+ and 0.044 M Fe2+
Ksp (CuS) = 1.3 × 10-36
Ksp (FeS) = 6.3 × 10-18
Step 2: Calculate precipitate
CuS → Cu^2+ + S^2- Ksp= 1.3*10^-36
FeS → Fe^2+ + S^2- Ksp= 6.3*10^-18
Calculate the minimum of amount needed to form precipitates:
Q=Ksp
<u>For copper</u> we have: Ksp=[Cu2+]*[S2-]
Ksp (CuS) = 1.3*10^-36 = 0.036M *[S2-]
[S2-]= 3.61*10^-35 M
<u>For Iron</u> we have: Ksp=[Fe2+]*[S2-]
Ksp(FeS) = 6.3*10^-18 = 0.044M*[S2-]
[S2-]= 1.43*10^-16 M
CuS will form precipitates before FeS., because only 3.61*10^-35 M Sulfur Ions are needed for CuS. For FeS we need 1.43*10^-16 M Sulfur Ions which is much larger.
The precipitate is CuS.
Sulfide will precipitate at [S2-]= 3.61*10^-35 M
Answers:
1. 3-ethyl-3-methylheptane; 2. 2,2,3,3-tetramethylpentane; 3. hexa-2,4-diene.
Explanation:
<em>Structure 1
</em>
- Identify and name the longest continuous chain of carbon atoms (the main chain has 7 C; ∴ base name = heptane).
- Identify and name all the substituents [a 1C substituent (methyl) and a 2C substituent (methyl).
- Number the main chain from the end closest to a substituent.
- Identify the substituents by the number of the C atom on the main chain. Use hyphens between letters and numbers (3-methyl, 3-ethyl).
- Put the names of the substituents in alphabetical order in front of the base name with no spaces (3-ethyl-3-methylheptane)
<em>Structure 2</em>
- 5C. Base name = pentane
- Four methyl groups.
- Number from the left-hand end.
- If there is more than one substituent of the same type, identify each substituent by its locating number and use a multiplying prefix to show the number of each substituent. Use commas between numbers (2,2,3,3-tetramethyl).
- The name is 2,2,3,3-tetramethylpentane.
<em>Structure 3
</em>
- Identify and name the longest continuous chain of carbon atoms that passes through as many double bonds as possible. Drop the <em>-ne</em> ending of the alkane to get the root name <em>hexa-</em>.
- (No substituents).
- Number the main chain from the end closest to a double bond.
- If there is more than one double bond use a multiplying prefix to indicate the number of double bonds (two double bonds = diene) and use the smaller of the two numbers of the C=C atoms as the double bond locators (2,4-diene)
- Put the functional group name at the end of the root name (hexa-2,4-diene).
<em>Note</em>: The name 2,4-hexadiene is <em>acceptable</em>, but the <em>Preferred IUPAC Name</em> puts the locating numbers as close as possible in front of the groups they locate.